Spider venom peptides as potential drug candidates due to their anticancer and antinociceptive activities
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | The Journal of venomous animals and toxins including tropical diseases (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1678-91992019000100203 |
Resumo: | Abstract Spider venoms are known to contain proteins and polypeptides that perform various functions including antimicrobial, neurotoxic, analgesic, cytotoxic, necrotic, and hemagglutinic activities. Currently, several classes of natural molecules from spider venoms are potential sources of chemotherapeutics against tumor cells. Some of the spider peptide toxins produce lethal effects on tumor cells by regulating the cell cycle, activating caspase pathway or inactivating mitochondria. Some of them also target the various types of ion channels (including voltage-gated calcium channels, voltage-gated sodium channels, and acid-sensing ion channels) among other pain-related targets. Herein we review the structure and pharmacology of spider-venom peptides that are being used as leads for the development of therapeutics against the pathophysiological conditions including cancer and pain. |
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The Journal of venomous animals and toxins including tropical diseases (Online) |
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|
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Spider venom peptides as potential drug candidates due to their anticancer and antinociceptive activitiesspider venom peptidesantitumorpaindrug candidatesAbstract Spider venoms are known to contain proteins and polypeptides that perform various functions including antimicrobial, neurotoxic, analgesic, cytotoxic, necrotic, and hemagglutinic activities. Currently, several classes of natural molecules from spider venoms are potential sources of chemotherapeutics against tumor cells. Some of the spider peptide toxins produce lethal effects on tumor cells by regulating the cell cycle, activating caspase pathway or inactivating mitochondria. Some of them also target the various types of ion channels (including voltage-gated calcium channels, voltage-gated sodium channels, and acid-sensing ion channels) among other pain-related targets. Herein we review the structure and pharmacology of spider-venom peptides that are being used as leads for the development of therapeutics against the pathophysiological conditions including cancer and pain.Centro de Estudos de Venenos e Animais Peçonhentos (CEVAP/UNESP)2019-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1678-91992019000100203Journal of Venomous Animals and Toxins including Tropical Diseases v.25 2019reponame:The Journal of venomous animals and toxins including tropical diseases (Online)instname:Universidade Estadual Paulista (UNESP)instacron:UNESP10.1590/1678-9199-jvatitd-14-63-18info:eu-repo/semantics/openAccessWu,TingWang,MengWu,WenfangLuo,QianxuanJiang,LipingTao,HuaiDeng,Meichuneng2019-07-04T00:00:00Zoai:scielo:S1678-91992019000100203Revistahttp://www.scielo.br/jvatitdPUBhttps://old.scielo.br/oai/scielo-oai.php||editorial@jvat.org.br1678-91991678-9180opendoar:2019-07-04T00:00The Journal of venomous animals and toxins including tropical diseases (Online) - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Spider venom peptides as potential drug candidates due to their anticancer and antinociceptive activities |
title |
Spider venom peptides as potential drug candidates due to their anticancer and antinociceptive activities |
spellingShingle |
Spider venom peptides as potential drug candidates due to their anticancer and antinociceptive activities Wu,Ting spider venom peptides antitumor pain drug candidates |
title_short |
Spider venom peptides as potential drug candidates due to their anticancer and antinociceptive activities |
title_full |
Spider venom peptides as potential drug candidates due to their anticancer and antinociceptive activities |
title_fullStr |
Spider venom peptides as potential drug candidates due to their anticancer and antinociceptive activities |
title_full_unstemmed |
Spider venom peptides as potential drug candidates due to their anticancer and antinociceptive activities |
title_sort |
Spider venom peptides as potential drug candidates due to their anticancer and antinociceptive activities |
author |
Wu,Ting |
author_facet |
Wu,Ting Wang,Meng Wu,Wenfang Luo,Qianxuan Jiang,Liping Tao,Huai Deng,Meichun |
author_role |
author |
author2 |
Wang,Meng Wu,Wenfang Luo,Qianxuan Jiang,Liping Tao,Huai Deng,Meichun |
author2_role |
author author author author author author |
dc.contributor.author.fl_str_mv |
Wu,Ting Wang,Meng Wu,Wenfang Luo,Qianxuan Jiang,Liping Tao,Huai Deng,Meichun |
dc.subject.por.fl_str_mv |
spider venom peptides antitumor pain drug candidates |
topic |
spider venom peptides antitumor pain drug candidates |
description |
Abstract Spider venoms are known to contain proteins and polypeptides that perform various functions including antimicrobial, neurotoxic, analgesic, cytotoxic, necrotic, and hemagglutinic activities. Currently, several classes of natural molecules from spider venoms are potential sources of chemotherapeutics against tumor cells. Some of the spider peptide toxins produce lethal effects on tumor cells by regulating the cell cycle, activating caspase pathway or inactivating mitochondria. Some of them also target the various types of ion channels (including voltage-gated calcium channels, voltage-gated sodium channels, and acid-sensing ion channels) among other pain-related targets. Herein we review the structure and pharmacology of spider-venom peptides that are being used as leads for the development of therapeutics against the pathophysiological conditions including cancer and pain. |
publishDate |
2019 |
dc.date.none.fl_str_mv |
2019-01-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1678-91992019000100203 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1678-91992019000100203 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/1678-9199-jvatitd-14-63-18 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Centro de Estudos de Venenos e Animais Peçonhentos (CEVAP/UNESP) |
publisher.none.fl_str_mv |
Centro de Estudos de Venenos e Animais Peçonhentos (CEVAP/UNESP) |
dc.source.none.fl_str_mv |
Journal of Venomous Animals and Toxins including Tropical Diseases v.25 2019 reponame:The Journal of venomous animals and toxins including tropical diseases (Online) instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
The Journal of venomous animals and toxins including tropical diseases (Online) |
collection |
The Journal of venomous animals and toxins including tropical diseases (Online) |
repository.name.fl_str_mv |
The Journal of venomous animals and toxins including tropical diseases (Online) - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
||editorial@jvat.org.br |
_version_ |
1748958540548014080 |